ANNOVAR	https://annovar.openbioinformatics.org/
Bureau international d’audiophonologie (BIAP)	https://www.biap.org/en/recommandations/recommendations/tc-02-classification
ClinVar	https://www.ncbi.nlm.nih.gov/clinvar/
dbNSFP (including dbscSNV)	https://sites.google.com/site/jpopgen/dbNSFP
dbSNP	https://www.ncbi.nlm.nih.gov/snp/
DRAGEN germline pipeline	https://emea.illumina.com/products/by-type/informatics-products/basespace-sequence-hub/apps/edico-genome-inc-dragen-germline-pipeline.html
Ensembl	https://www.ensembl.org/index.html
Gene ontology (GO)	http://geneontology.org/
Genome aggregation database (gnomAD)	https://gnomad.broadinstitute.org/
Genome analysis toolkit (GATK)	https://gatk.broadinstitute.org/hc/en-us
Hereditary hearing loss homepage (HHL)	https://hereditaryhearingloss.org/
Human phenotype ontology (HPO)	https://hpo.jax.org/app/
Human splice finder (HSF)	https://hsf.genomnis.com/home
InterProScan	http://www.ebi.ac.uk/InterProScan/
MODELLER	http://www.salilab.org/modeller
NCBI-BLAST	https://blast.ncbi.nlm.nih.gov/Blast.cgi
Online Mendelian inheritance in man (OMIM)	https://omim.org/
PDB	https://www.wwpdb.org/
PSIPRED	http://bioinf.cs.ucl.ac.uk/psipred/
PYMOL	http://www.pymol.org/
RefSeq	https://www.ncbi.nlm.nih.gov/refseq/
Swiss-Model	https://swissmodel.expasy.org/
Uniprot	https://www.uniprot.org/uniprot/Q9NZA1
UK10K	https://www.uk10k.org/
World Health Organisation	https://www.who.int/news-room/fact-sheets/detail/deafness-and-hearing-loss